BEUDAMED
    FDA Adverse Event Other Summary report: N

    ABBOTT

    MDR report key: 252050 · Received November 19, 1999

    Report

    Report Number
    252050
    Event Type
    Other
    Date Received
    November 19, 1999
    Date of Event
    October 29, 1999
    Report Date
    November 19, 1999
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    JHI
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PT WAS HAVING PRE-OPERATIVE BLOOD WORK FOR SURGERY. AFTER RECEIVING THE TEST RESULT THE SURGEON CANCELLED THE SURGICAL PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT AXSYM JHI ABBOTT LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 18 YR Other